6063 results about "Hydroxy group" patented technology

An aqueous ultraviolet-absorbing resin emulsion, and an aqueous resin emulsion composition containing the emulsion is provided, wherein the emulsion is excellent in compatibility with a synthetic resin and light resistance. Also, the emulsion improves stability in blending with an aqueous emulsion of the synthetic resin, and prevents bleed out of the ultraviolet-absorbing resin on the surface of a coating film. Further, the aqueous ultraviolet-absorbing resin emulsion imparts excellent alkali or solvent resistance to a synthetic resin poor in alkali or solvent resistance. More specifically, an aqueous resin emulsion composition comprising (I) an aqueous ultraviolet-absorbing resin emulsion and (II) an other aqueous resin emulsion is provided, wherein the emulsion (I) is obtained by urethanizing (A) a polyol component having an ultraviolet-absorbing group {e.g., 1,1-bis[3-(2H-benzotriazol-2-yl)-4-hydroxy-benzeneethanol]methane}, (B) a polyol if necessary, (C) an alkyl or aryl dialkanolamine compound, and (D) an organic polyisocyanate in (E) an organic solvent, diluting the reaction mixture with (F) an organic solvent having a boiling point lower than 100° C. to give a resin solution, neutralizing the resin solution with (G) a neutralizing agent, and dispersing the resultant in water.

The invention discloses a supported nickel catalyst for preparing 1, 3-propylene glycol through hydrogenation of 3-hydroxypropionaldehyde as well as a preparation method and application of the supported nickel catalyst, and relates to the technical field of catalysts. The modified long-chain multi-carbon inducer is used, and a special long-chain molecular structure and a branched chain group of the inducer can effectively and selectively adsorb and occupy a micropore impregnation site; the preparation method has the beneficial effects that more active component nickel species are obviously promoted to be dispersed in main reaction confinement spaces such as mesopores and macropores and interact with the carrier to form effective active sites, and active component steeping liquor is inhibited from entering micropore channels due to capillary action; the active site failure caused by agglomeration of nickel species in micropores in the subsequent drying and roasting process of the catalyst precursor is avoided, the efficient and directional reaction is ensured, the generation of by-products is greatly reduced, the pressure is relieved for the subsequent product rectification separation, and the final product purity is improved. The catalyst provided by the invention can still keep an excellent catalytic effect when the air speed of a 3-hydroxypropionaldehyde solution is increased to 6.5 h <-1 >.

The invention provides a hydroxytyrosol supramolecular compound and a preparation method and application thereof, and belongs to the technical field of cosmetics and biological medicine, the supramolecular compound comprises the following chemical components by mass: 0.01-10% of hydroxytyrosol, 2-45% of an amino acid compound, 2-20% of alpha hydroxy acid, 2-30% of urea, and 15-92% of water. The supramolecular compound can promote transdermal delivery of hydroxytyrosol and maintain the biological activity of hydroxytyrosol, shows high biocompatibility, and can be applied to product development in the antibacterial field, the regeneration field and the anti-aging field.

The invention discloses a dynamic borate bond-based self-healing polyacrylic acid binder and a preparation method thereof. The dynamic borate bond-based self-healing polyacrylic acid binder comprises a polymer main chain and a dynamic cross-linking agent, the dynamic cross-linking agent is a polyol compound containing at least two pairs of ortho-hydroxyl groups; the polymer main chain is formed by copolymerizing the following monomers: an acrylic structural monomer, the molar fraction of which accounts for 85-94% of the total monomer; a functional monomer containing a boric acid group, wherein the molar fraction of the functional monomer accounts for 3-8% of the total monomer; the mole fraction of the flexible monomer containing the acrylate group accounts for 3-8% of the total monomer. Various stresses generated by different negative electrode materials in circulation can be effectively adapted and buffered through a network formed by dynamic boric acid ester bonds and reversible fracture and combination of the boric acid ester bonds, so that the service life of the battery is generally prolonged, the working temperature range of the battery can be remarkably widened, the low-temperature discharge capacity can be remarkably increased, and the high-temperature cycle life can be prolonged.

S-Beta-hydroxybutyric acid compositions for oral delivery are effective in rapidly raising blood ketone levels without causing acute acidosis or gastrointestinal (GI) distress when consumed in sufficiently dilute form and / or as a gel or suspension. By limiting added beta-hydroxybutyrate salts containing alkali or alkaline earth metal ions, beta-hydroxybutyric acid solutions, gels, or suspensions can deliver exogenous ketone bodies without significantly altering electrolyte balance. Although aqueous beta-hydroxybutyric acid solutions are moderately acidic with a pH of about 3.5 to 4, when diluted with sufficient water, the water acts as a pseudo buffering agent that offsets otherwise harsh acidic effects when consumed orally. Gels and suspensions can also ameliorate acidic effects by partially encapsulating the beta-hydroxybutyric acid. Beta-hydroxybutyric acid can be pure S-beta-hydroxybutyric acid or a non-racemic mixture enriched with S-beta-hydroxybutyric acid relative to R-beta-hydroxybutyric acid.

The invention provides a bio-based 1, 4-butanediol composition as well as a preparation method and application thereof, and the bio-based 1, 4-butanediol composition comprises bio-based 1, 4-butanediol, 4-hydroxybutyric acid-(4-hydroxyl) butyl ester and bis (4-hydroxyl) dibutyl ether. The total mass content of 4-hydroxybutyric acid-(4-hydroxyl) butyl ester and bis (4-hydroxyl) dibutyl ether in the bio-based 1, 4-butanediol composition is 51 to 220 ppm. The bio-based 1, 4-butanediol composition has low hygroscopicity, and can maintain low water content after long-term storage; meanwhile, when the bio-based 1, 4-butanediol composition is used for polyester synthesis, the esterification time can be shortened, the reaction efficiency can be improved, side reactions can be reduced, and a polyester product with better damp-heat resistance stability can be obtained.

Compositions for delivering ketone bodies to a subject include one or more beta-hydroxybutyrate salts, one or more acetoacetate salts, beta-hydroxybutyric acid, and optionally acetoacetic acid. The compositions may optionally include one or more ketone body esters, such as one or more beta-hydroxybutyrate esters and / or one or more acetoacetate esters. An example composition contains about 2% to about 98% on a molar basis of the one or more beta-hydroxybutyrate salts and the one or more acetoacetate salts, about 2% to about 98% on a molar basis of the beta-hydroxybutyrate free acid and optionally the acetoacetate free acid, and optionally about 2% to about 98% on a molar basis of one or more ketone body esters.

The invention discloses a preparation method of 5-hydroxy-3-iminopyridine-2, 6-diketone, and relates to the technical field of compound preparation. The invention provides a preparation method of 5-hydroxy-3-iminopyridine-2, 6-diketone, which comprises the following steps: uniformly mixing observation blue with at least one oxidant of sodium hypochlorite, potassium permanganate and hydrogen peroxide according to a molar ratio of 1: (0.5-1.5) under a solution condition, reacting for 5-120 minutes, and adding a reducing agent to finish the reaction, thereby obtaining a target product. According to the preparation method provided by the invention, on the basis of the amide structure of the ornamental blue, 'endogenous catalysis' of the reaction can be realized, no additional catalyst needs to be introduced, and the 5-hydroxy-3-iminopyridine-2, 6-diketone with the yield of more than 60.53% and the purity of more than 60.2% can be prepared through a simple and convenient one-step reaction.

The invention relates to the technical field of fuels and additives thereof, in particular to an alcohol fuel with a catalytic effect and an additive thereof.The alcohol fuel with the catalytic effect comprises C1-C7 alcohol and hydrocarbon, and a rare earth compound catalytic material is used in the fuel; the rare earth compound comprises a hydroxyl group or a phenyl group or a C5-C25 group or a carboxyl group or an amino group or a metal, the alcohol fuel is high in formula calorific value adjustable calorific value, can well adapt to an internal combustion engine or an engine for testing the alcohol fuel, is a novel alternative energy with potential, and can be used for preparing the alcohol fuel. The environmental protection problem of fossil fuel is solved, and the fuel efficiency is accelerated.

The invention discloses a preparation method of a rubber waterstop material with a low compression set rate, which comprises the following steps: firstly, carrying out blending reaction on hydroxyl silicone oil and boric acid to obtain liquid polyborosiloxane; the preparation method comprises the following steps: adding liquid polyborosiloxane and natural rubber into an internal mixer according to a ratio, and carrying out internal mixing to obtain a mixture; adding zinc oxide, an anti-aging agent, stearic acid and an anti-tearing agent into the obtained mixture, and continuously mixing; continuously adding kaolin talcum powder, calcium carbonate, calcium oxide, white carbon black, N550, N330 and KH550, and internally mixing again to obtain a preform; adding a vulcanization accelerator and a vulcanizing agent into the preform, and continuously mixing to obtain a rubber material to be vulcanized; and vulcanizing and forming the rubber material to be vulcanized to prepare the rubber water-stop belt material with the low compression set rate. According to the invention, the compression set rate of the rubber material can be reduced while the tensile strength, elongation, tear resistance and other properties of the rubber are not sacrificed, so that the product performance is enhanced.

The invention provides polyester and a preparation method and application thereof, the polyester comprises a structural unit derived from the following monomer components: at least one monomer component I selected from hydroxybenzoic acid or hydroxynaphthoic acid; and at least one monomer component II, wherein the monomer component II is selected from p-hydroxybenzoic acid containing a substituent group. A small amount of the monomer component II is introduced into the polyester material, interaction points are provided for chain segments of the polymer, the chain segments are promoted to form a branched structure, and therefore the melt strength of the polymer is well improved.

The invention provides a preparation method for preparing porous carbon based on an aerogel method, the porous carbon and application of the porous carbon, and belongs to the technical field of porous carbon material preparation. The preparation method comprises the following steps: mixing polyhydroxy phenol, aromatic aldehyde, acrylamide, graphene oxide and lithium salt according to a mass ratio of 100: (50-200): (5-30): (1-5): (1-5), carrying out hydrothermal reaction at 100-200 DEG C for 1-6 hours, and freeze-drying at-40 DEG C to obtain a hydrogel precursor; and carbonizing the precursor in organic heteroatom gas at 500-800 DEG C, mixing the intermediate with alkali according to the ratio of 100: (100-500), activating at 900-1100 DEG C, pickling and drying to obtain the porous carbon. The conductivity of the product is improved by means of graphene, lithium salt and heteroatoms, and the aerogel method obtains large aperture, has the characteristics of low impedance, high first efficiency and small charge-discharge expansion, and can be efficiently applied to silicon-carbon materials.

The invention provides a washable stable humidity-sensitive printing paste composition, a humidity-sensitive printing paste and a preparation method and application thereof. The washing-resistant stable humidity-sensitive printing paste composition comprises humidity-sensitive resin, an interface anchoring agent, a rheology modifier, a latent cross-linking agent and water, the humidity-sensitive resin contains amino and / or hydroxyl, and the latent cross-linking agent is selected from oxime-terminated alicyclic polyisocyanates or derivatives thereof. The latent cross-linking agent has chemical inertness at room temperature and can ensure the rheological stability of the slurry in the printing process, in the baking process, an end-capping reagent in the latent cross-linking agent is dissociated, an isocyanate group and amino and / or hydroxyl in the humidity-sensitive resin are subjected to a cross-linking reaction to form a semi-interpenetrating network structure, and the structure allows water molecules to enter and exit, so that the moisture-sensitive printing ink is formed. The fabric has the humidity-sensitive response characteristic, excessive swelling and movement of hydrophilic chain segments can be limited, dissociation or falling of humidity-sensitive resin under the action of washing shearing force is prevented, and the humidity-sensitive characteristic and washing-resistant stability are improved.

The invention provides LED-UV (Light Emitting Diode-Ultraviolet) curing ink as well as a preparation method and application thereof, and the LED-UV curing ink is prepared from the following components in parts by weight: 30 to 50 parts of modified polyurethane acrylate resin, 15 to 30 parts of modified epoxy acrylate resin, 10 to 15 parts of amino resin, 15 to 30 parts of acrylate monomer, 6 to 10 parts of photoinitiator, 1 to 3 parts of adhesion promoter, 2 to 4 parts of coupling agent, 0.5 to 1 part of defoaming agent and 1 to 2 parts of flatting agent. The modified polyurethane acrylate resin is hydroxyl and / or carboxyl modified polyurethane acrylate resin; the modified epoxy acrylate resin is polyurethane modified epoxy acrylate resin. After the ink is photo-cured, a paint film has good flexibility, adhesive force and chemical resistance; the hardness, the curing speed and the chemical resistance of a paint film can be improved; the adhesive force to a base material can be promoted; and the water resistance and the wine soaking resistance of a paint film are enhanced.

The invention discloses an electrolytic solution of a platinum-rhodium alloy, a preparation method and a preparation method of a plating layer of the platinum-rhodium alloy, and belongs to the technical field of precise electroplating. The electrolytic solution comprises a platinum salt, a rhodium salt, a first additive, a second additive, a first complexing agent, a second complexing agent, a first stabilizer and a second stabilizer, the first additive is a sulfamic acid compound containing 3-4 hydroxyalkyl groups, the second additive is sulfamic acid salt containing 3-4 hydroxyalkyl groups, and the first complexing agent and the second complexing agent are a platinum salt and a rhodium salt. The first complexing agent is a mixture of dicarboxylic acid and dicarboxylic acid containing amino or hydroxyl, the second complexing agent is a salt corresponding to the dicarboxylic acid, and the first stabilizer is a mixture of alkyl sulfonic acid and alkyl sulfonate. Through the synergistic effect of the additive, the complexing agent and the stabilizer, the additive, the complexing agent and the stabilizer form a five-membered to seven-membered heterocyclic coupling structure with platinum ions and rhodium ions, and the stability of the electrolytic solution is remarkably improved. And the obtained platinum-rhodium alloy coating is compact and uniform, and has excellent nitric acid steam and mixed gas corrosion resistance.

The invention discloses a single-component high-heat-resistance type epoxy adhesive and a preparation method of the single-component high-heat-resistance type epoxy adhesive. The adhesive is prepared from the following components in parts by weight: 30 to 40 parts of N, N-4, 4 '-diphenylmethane bismaleimide; 50 parts of bisphenol F epoxy resin; 36.47 parts of 4, 4 '-diaminodiphenyl sulfone; 20 to 40 phr of phenyl glycidyl ether; 1 to 2 phr of two terminal type epoxy silicone oil; 4 to 6 phr of hydroxyl-terminated polyether sulfone; 10 to 20 phr of boron nitride, the surface of which is modified by gamma-glycidyl ether oxypropyl trimethoxy silane; and 1 to 3 phr of an adhesion promoter. According to the adhesive disclosed by the invention, the heat resistance, the mechanical property, the dimensional stability, the process adaptability and the like are synergistically improved, the use requirements of an aviation structural part on long-term service at 150-180 DEG C and an electronic packaging device on the condition of short-time reflow soldering at about 200 DEG C can be met, and the reliability of the adhesive in a high-temperature environment is remarkably improved.

The invention discloses a high-performance polypropylene material and a preparation method thereof, and belongs to the technical field of high-performance polypropylene, the high-performance polypropylene material is characterized by being prepared from the following components by weight: 50-80 parts of polypropylene, 10-30 parts of inorganic ultrafine particle coated talcum powder, 5-20 parts of a flexibilizer, 2-5 parts of a dispersant, 0.2-0.5 part of an antioxidant, and 0.5-3 parts of a nucleating agent. The invention has the following beneficial effects: the material with excellent comprehensive mechanical properties such as notch impact strength, tensile strength and bending strength is obtained; the inorganic ultrafine particle coated talcum powder has excellent dispersity to form an effective'coating 'or'filling' structure, and also has firm Si-O-Si covalent bonds formed with hydroxyl groups on the surface of the filler, so that the comprehensive performance of the material is improved.

The invention belongs to the technical field of hydrometallurgy, and particularly relates to a method for separating nickel and cobalt from a nickel-containing solution and preparing nickel salt, which comprises the following steps: 1) chelating and precipitating impurity metal ions in the nickel-containing solution by using ammonium polyphosphate with the polymerization degree of more than 1000 as an impurity removal agent, thereby removing copper, iron, zinc and aluminum to obtain an impurity-removed solution; 2) extracting the impurity-removed solution by using a diluent, alpha-hydroxyoxime, carboxylic acid and alkyl alcohol as an extraction organic phase to obtain a nickel-loaded organic phase; 3) washing the nickel-loaded organic phase by using nickel-containing washing water; and (4) reverse extraction is conducted on the washed nickel-loaded organic phase through reverse extraction liquid containing acid and nickel ions, nickel-rich liquid is obtained after reverse extraction is completed, nickel salt in the nickel-rich liquid is crystallized, and nickel salt solids are obtained after phase separation. According to the method, nickel is selectively extracted through the compound extraction system after impurity removal, the extraction rate of nickel reaches up to 99.8%, nickel is separated from metal ions such as cobalt and lithium, and the method is simple in process, low in equipment manufacturing cost and low in manufacturing cost.

The invention discloses a low-viscosity ternary eutectic solvent as well as a preparation method and application thereof, and belongs to the technical field of CO2 absorbents. The low-viscosity ternary eutectic solvent is composed of polyamine hydrochloride, steric hindrance amine and organic alcohol, the polyamine hydrochloride has multiple active amino groups and is used for guaranteeing the high CO2 absorption rate and absorption load of the ternary eutectic solvent, the steric hindrance amine can inhibit formation of a hydrogen bond network due to the unique steric hindrance structure, and the high CO2 absorption rate and absorption load of the ternary eutectic solvent are improved. The organic alcohol can be used as a viscosity regulating agent, active hydroxyl of the organic alcohol can promote proton transfer in a CO2 desorption reaction, and the CO2 desorption efficiency is enhanced. The ternary eutectic solvent provided by the invention can still maintain a low-viscosity homogeneous liquid state after absorbing CO2, can effectively reduce the reduction of mass transfer efficiency caused by high viscosity, influence on contact with a target compound, heat transfer efficiency and the like, and solves the ubiquitous problems of overhigh viscosity and insufficient regeneration efficiency of the existing DESs system.

The present invention relates to detergents and cleaning compositions that comprise a surfactant, an anti-redeposition agent, and an effective amount of 1,2-heptanediol and / or 2,3-heptanediol or a specific type of anti-redeposition boosting agent, such as alkanediols, glyceryl caprylate, 4-hydroxyacetophenone, ethyl hexyl glycerin or tropolone, and the use of said detergents and cleaning compositions for the preparation of a detergent and cleaning product for household, institutional and industrial application. Furthermore, the present invention relates to a method of treating a stained and / or soiled substrate, using the detergents and cleaning compositions according to the present invention. Additionally, the present invention relates to the use of 1,2-heptanediol and / or 2,3-heptanediol or of specific substances as defined herein for boosting the activity of an anti-redeposition agent in a detergent and cleaning composition and / or for improving cleaning performance of a detergent and cleaning composition. Moreover, the present invention relates to a method of boosting the activity of an anti-redeposition agent in a detergent and cleaning composition and / or of improving cleaning performance of a detergent and cleaning composition by adding an effective amount of 1,2-heptanediol and / or 2,3-heptanediol or of specific anti-redeposition agents, such as alkanediols, glyceryl caprylate, 4-hydroxyacetophenone, ethyl hexyl glycerin or tropolone to said detergent and cleaning composition. Finally, the present invention relates to the use of 1,2-heptanediol, 2,3-heptanediol or a mixture comprising 1,2-heptanediol and 2,3-heptanediol or at least one anti-redeposition boosting agent, such as alkanediols, glyceryl caprylate, 4-hydroxyacetophenone, ethyl hexyl glycerin or tropolone as anti-redeposition agent.

The invention relates to a starch pore-enlarging type high-chlorine-capacity long-acting high-temperature dechlorinating agent and a preparation method thereof, and belongs to the technical field of dechlorinating, the starch pore-enlarging type high-chlorine-capacity long-acting high-temperature dechlorinating agent comprises the following raw materials: complexing coating calcium hydroxide, modified hydroxyapatite, a composite inorganic adhesive, reinforcing and toughening whiskers, a composite pore-forming agent, a composite synergist, nano calcium carbonate and water; according to the starch reaming type high-chlorine-capacity long-acting high-temperature dechlorinating agent obtained by the invention, the breakthrough chlorine capacity is 40.9 to 44.9 percent, the crushing strength is 139 to 151N. Cm <-1 >, and the abrasion rate is 0.8 to 1.5 percent.

The invention relates to a method for preparing lithium phosphate from a lithium-containing solution by using an extraction-reverse extraction technology, an extraction agent adopted in the method comprises a main extraction agent, a synergistic extraction agent and a diluent, the pKa value of the main extraction agent is greater than 12.5, the synergistic extraction agent has a P = O group, a hydroxyl group or a cavity diameter of 0.12-0.15 nm, the water solubility of the synergistic extraction agent is less than or equal to 50 mg / L, the viscosity is less than or equal to 50 mpa.s, and the diluent is a diluent. The synergistic extraction factor R of the extraction agent is more than 100, R = Dmix / (D1 + D2), the Dmix is the extraction distribution ratio of the main extraction agent to lithium when the main extraction agent and the synergistic extraction agent are mixed according to the mass ratio of (1: 1)-(1: 2), the D1 is the extraction distribution ratio of the main extraction agent to lithium, the D2 is the extraction distribution ratio of the synergistic extraction agent to lithium, and the stripping agent is phosphoric acid. According to the method disclosed by the invention, by selecting the main extraction agent and the synergistic extraction agent, on one hand, lithium monohydrogen phosphate and lithium dihydrogen phosphate impurities cannot be generated by reaction when phosphoric acid is adopted for reverse extraction, and on the other hand, sodium and potassium can be separated at a higher degree during extraction, so that high-purity lithium phosphate can be efficiently prepared.

The invention relates to the technical field of high-molecular polymers, and particularly discloses a polyimide adhesive for high-temperature adhesion as well as a preparation method and application of the polyimide adhesive. The polyimide adhesive is prepared from the following raw materials in parts by mole: a diamine compound with a polyhydroxy structure, a flexible dianhydride compound, an organic solvent, a dehydrating agent and a catalyst, the preparation method comprises the following steps: dissolving a diamine compound in an organic solvent, adding a dianhydride compound, reacting to generate a polyimide precursor, adding a dehydrating agent and a catalyst, and reacting to generate the polyimide adhesive. The polyimide adhesive for high-temperature bonding can be applied to bonding of metal materials, ceramic materials and glass materials, and has the advantages of high bonding force, excellent high-temperature resistance, better chemical stability and capability of resisting acid and alkali erosion.

The invention discloses a preparation method of 3, 6-dichloropyridazine, and belongs to the technical field of chemistry. According to the method, 3, 6-dihydroxypyridazine is used as a raw material, an organic solvent and triphenylphosphine oxide are combined to form a dichlorotriphenylphosphine intermediate state which is used as a chlorinating agent, dihydroxyl is substituted to generate 3, 6-dichloropyridazine, triphenylphosphine oxide and solid light are used as raw materials, heating reaction is performed to prepare 3, 6-dichloropyridazine, meanwhile, a one-pot method can be adopted in the two-step reaction, and operation is easy and convenient. The novel preparation method for synthesizing 3, 6-dichloropyridazine provided by the invention has the advantages of low raw material cost, high yield, high gas phase purity and no pollution, is suitable for industrial production, can meet industrial requirements, provides a new idea for later preparation of 3, 6-dichloropyridazine, has the remarkable advantages of high gas phase purity and high yield, and is suitable for industrial production. Wide application prospects are realized.

The invention belongs to the technical field of organic synthesis, and provides a preparation method of a cationic lipid compound, which comprises the following steps: (1) reacting 1, 5-dihalopentane, 2-tert-butyl glycolate and alkali to obtain a product G; (2) hydrolyzing the product G under an acidic condition to obtain a product H; (3) carrying out esterification reaction on the product H, the raw material C, 4-dimethylaminopyridine and a condensing agent in dichloromethane to obtain a product J; and (4) carrying out amination reaction on the product J, the raw material L and alkali in acetonitrile to obtain the cationic lipid compound. Compared with the prior art, the method has the relatively remarkable advantages that when the first part of halogenated long-chain alkyl ester H is synthesized by the method, 1, 5-dihalopentane and 2-tert-butyl glycolate are used as raw materials, the halogenated long-chain alkyl ester J is synthesized by a simple method, the product is obtained at a higher yield in synthesis, and the method is suitable for kilogram-level production. The route synthesis only comprises four steps of chemical reactions, and is suitable for industrial production.

The invention discloses a tubular continuous flow preparation process and a tubular continuous flow preparation device for (R)-(+)-2-(4-hydroxyphenoxy) propionic acid. A hydroquinone aqueous solution and a sodium hydroxide solution are respectively preheated and mixed, and then enter a tubular reactor I for reaction to obtain a hydroquinone sodium alkaline solution. And pumping (S)-(-)-2-methyl chloropropionate into a reaction system, respectively preheating the (S)-(-)-2-methyl chloropropionate and the hydroquinone sodium alkaline solution obtained in the previous step, mixing the (S)-(-)-2-methyl chloropropionate and the hydroquinone sodium alkaline solution, carrying out nucleophilic substitution reaction in a tubular reactor II, and carrying out post-treatment on the reaction completion solution to obtain the high-purity (R)-(+)-2-(4-hydroxyphenoxy) propionic acid. According to the method, an optimization method combining a tubular reaction technology and kinetic research is adopted, and MATLAB simulation and experimental verification are combined, so that the reaction yield reaches 95% or above, and the purity reaches 99% or above; the method is high in reaction controllability, fully continuous in reaction process, convenient to operate, low in cost and suitable for industrial production, and the use amount of hydroquinone is greatly reduced.

The present invention relates to a dental diaphragm copolyester and a preparation method thereof, the preparation method comprises the following steps: 2, 5-furandicarboxylic acid or an ester thereof, aliphatic or alicyclic diol and (2-hydroxy-5-formyl phenyl) diphenylborane are subjected to a reaction to obtain an esterification or ester exchange product; and carrying out condensation polymerization on the esterification or ester exchange product and the stabilizer to prepare the copolyester for the dental diaphragm. 2, 5-furandicarboxylic acid is derived from a renewable biomass resource and meets the requirements of green and sustainable development; compared with terephthalic acid and furan ring structures, the film has higher rigidity and polarity, the yield of hot press molding is improved, the same correction force can be met by a thinner film, the wearing comfort of a patient is improved, and meanwhile stress relaxation is improved; the catalyst perfectly combines strong Lewis acidity, intramolecular stabilization and potential bifunctional activation through structural design, provides possibility for efficient and green synthesis of polyester, avoids use of heavy metal, and is higher in biological safety.

The invention discloses a preparation method and application of a catalyst based on pyridine ionic liquid, and belongs to the technical field of catalyst preparation. According to the invention, a hydrolysis reaction of a silane coupling agent is utilized to prepare a silicon oxide nanotube containing a pyridine unit, and then a quaternization reaction is carried out to obtain the catalyst based on the pyridine ionic liquid. The catalyst has a high specific surface area and a rich pore channel structure, exposure of active sites and contact of the active sites and reactants are facilitated, and the catalytic rate is increased. Meanwhile, the silicon oxide nanotube contains hydroxyl, and can cooperate with a pyridine ionic liquid site to catalyze a carbon dioxide cycloaddition reaction. The obtained catalyst can catalyze the reaction of carbon dioxide and an epoxy compound to prepare cyclic carbonate under solvent-free and metal-free conditions, and the catalyst is easy to recover and simple in product purification, and has a good application prospect.

The invention relates to the technical field of water treatment agents, and particularly discloses an anti-corrosion deoxidizing composite agent for geothermal well recharge water and a preparation method of the anti-corrosion deoxidizing composite agent. The invention relates to an anti-corrosion and deoxidizing composite agent for geothermal well recharge water. The anti-corrosion and deoxidizing composite agent comprises the following raw materials: 30-40 parts of double modified sodium sulfite, 10-20 parts of a corrosion inhibitor, 8-15 parts of a scale inhibitor, 5-10 parts of amino trimethylene phosphonic acid, 5-10 parts of etidronic acid, 3-8 parts of polyethylene glycol monomethyl ether acrylate and 40-50 parts of deionized water. The dual-modified sodium sulfite is obtained by sequentially modifying sodium sulfite with a silane coupling agent and acrylic acid. The corrosion-resistant and oxygen-removing composite agent has the advantage of being high in oxygen-removing efficiency stability, the corrosion-resistant and scale-inhibiting functions are synchronously and synergistically improved on the basis that the oxygen-removing efficiency stability is guaranteed, and the complex working condition requirements of geothermal well recharge are completely met.

The invention discloses a bio-based recoverable high-thermal-conductivity dynamic ordered network composite material and a preparation method thereof, and is characterized in that the material takes a bio-based multifunctional epoxy system and a carboxylic acid compound containing disulfide bonds as reaction monomers, and the reaction monomers are reacted under the conditions of high temperature and metal salt catalyzed epoxy-carboxylic acid esterification reaction to obtain the bio-based recoverable high-thermal-conductivity dynamic ordered network composite material. A dynamic ordered network structure simultaneously containing disulfide bonds and beta-hydroxyl ester bonds is constructed, and the dynamic ordered network can be used as a springboard for phonon transmission, serves as an efficient'thermal bridge ', and plays a role similar to an ordered'crystal domain', so that higher heat-conducting property is shown when heat-conducting filler is not introduced, high flexibility and intrinsic heat conduction are realized, and the service life of the material is prolonged. And the material is endowed with reprocessing and recycling characteristics. Due to the synergistic existence of carboxyl, hydroxyl generated by epoxy ring opening and metal coordination in the system, and in combination with electrostatic interaction, Van der Waals force and hydrophobic interaction, the material has the adhesion characteristic suitable for a thermal interface at the same time.